In this episode, we dive into a topic that so many parents of individuals with autism experience — caretaker fatigue. When the needs are constant and the demands feel never-ending, it’s easy for caregivers to put themselves last… until burnout sets in.

We talk about the signs and symptoms of caretaker fatigue and why prioritizing yourself is not selfish — it’s essential. Christi shares honestly about her experience raising Alec, including the ways she felt supported by friends, the moments she felt isolated, and the intentional choices she made to care for herself along the way.

We discuss why taking breaks — including trips without Alec — allowed Christi to reconnect with her other children, feel renewed, and return as a better, more present caregiver. Because the last thing any parent wants is to feel resentment toward the individual who needs their care.

This episode is a reminder that supporting an individual with autism starts with supporting the caregiver. When parents take care of themselves, everyone benefits — especially their child.

If you’re a parent or caregiver feeling stretched thin, this conversation is for you.

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In this episode, we talk openly about Alec’s journey with epilepsy over the last 12 years. Alec had his first seizure at 16, and like many individuals on the autism spectrum, epilepsy became an additional and life-changing diagnosis.

According to the Epilepsy Foundation, 20–30% of individuals with autism also have epilepsy, making seizures the most common neurologic complication associated with autism.

We share the realities of navigating the medical system, the frustration of not always being heard, and the long, difficult process of finding the right medication — one that not only controlled seizures but also minimized side effects. Those years were some of the hardest Alec has faced, and they shaped how we advocate, ask questions, and push for better care.

This episode is for families raising children on the spectrum who are also managing epilepsy or other medical complexities. We hope Alec’s story helps you feel less alone, more informed, and more empowered to advocate for your child.

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In this episode, we talk all about setting goals with Alec and why goal setting matters for everyone — on the autism spectrum or not. Every individual deserves to feel pride, confidence, and a sense of accomplishment, and for some, that journey simply requires additional support and structure.

Alec has been setting goals from a young age. We started small with attainable, short-term goals and gradually built toward larger, yearly goals that support independence, confidence, and growth. Along the way, we’ve learned how powerful it is to break goals into manageable steps and celebrate progress at every stage.

We share how we’ve adapted goal setting over time, what’s worked, what we’ve adjusted, and why helping individuals on the spectrum experience success is just as important as the goals themselves. Whether you’re supporting a young child, a teen, or an adult with autism, this episode offers encouragement and practical ideas to help make goal setting meaningful and achievable — piece by piece.

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In this episode, we’re recapping the holidays — autism and all. The holiday season can be especially challenging for individuals on the autism spectrum, with disrupted routines, sensory overload, and nonstop social demands. This year, we’re happy to report that Alec earned a solid B+, and we couldn’t be more thrilled.

We break down what worked well for Alec, the strategies that helped support him, and what we might do differently next time. While this holiday season felt like a win, it hasn’t always been this way — and we share openly about the years when the holidays were anything but successful.

This honest recap is meant to encourage families who are still in the trenches. Progress isn’t about perfection — it’s about learning, adjusting, and celebrating the small wins along the way. If your holidays felt hard, you’re not alone, and there is hope for smoother seasons ahead.

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Join us—Angie Matheney and Christi Jensen—for a candid Q&A-style conversation where Christi opens up about what she wishes she could have told her younger self when Alec was first diagnosed.

We talk about the shifting priorities that come with raising a child on the spectrum, the pressure to "do everything right," and the importance of giving yourself grace. Whether you're just starting out or years into your journey, this episode offers encouragement, perspective, and a reminder that you're not alone.

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In this episode, we’re talking chores—how we got Alec started, how we create chore chains with just the right level of support, and why these daily tasks are so much more than household responsibilities.

Chores have been a huge part of Alec’s journey toward independence. We share how we taught him to complete tasks step by step, how we adjusted support as his skills grew, and why we believe every child—regardless of ability—can take pride in contributing at home.

Chores also lay a solid foundation for real-world job skills. These early routines can turn into resume-worthy experience, and we’ve seen firsthand how powerful that can be.

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In this episode, we—Angie and Christi—look back on Alec’s early years and the start of our autism journey. We share what it was like when Alec was diagnosed at just 2 years old, some of the behaviors he struggled with, and how we navigated those early, uncertain days as parents and caregivers.

We talk about the professionals who came into our lives and played a huge role in shaping Alec’s progress, as well as the lessons we learned along the way. It’s a personal, emotional, and sometimes funny reflection on those formative years. If you're just beginning this path or have already walked it, we hope our stories bring comfort, hope, and maybe even a few laughs.

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In this episode, we dive into the real challenges families face during the holiday season when raising children on the autism spectrum. What should be a magical, joyful time can quickly turn stressful with disrupted routines, extra people in the house, sensory overload, travel, noise, and unpredictable schedules.

We talk about why the holidays can feel “not so merry and bright,” share our own experiences, and offer practical tips for reducing stress—for kids and parents. From preparing for transitions to managing big feelings, creating safe spaces, and setting realistic expectations, we explore ways to make the season more manageable and meaningful.

If your holidays don’t look like a Hallmark movie, you’re not alone—and this conversation is for you.

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